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  4. 63621-353
  5. NDC Package Code: 63621-353-65 Sundrops 67

NDC Package 63621-353-65 Sundrops 67

Chloroxylenol Soap Topical - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
63621-353-65
Package Description:
8 BAG in 1 BOX / 1000 mL in 1 BAG
Product Code:
63621-353
Proprietary Name:
Sundrops 67
Non-Proprietary Name:
Chloroxylenol
Substance Name:
Chloroxylenol
Usage Information:
Wet hands and forearms.Apply a small amount (5 mL) or palmful to hands and forearms.Scrub thoroughly for at least fifteen seconds.Rinse completely and dry.
11-Digit NDC Billing Format:
63621035365
NDC to RxNorm Crosswalk:
  • RxCUI: 1045003 - chloroxylenol 0.75 % Medicated Liquid Soap
  • RxCUI: 1045003 - chloroxylenol 7.5 MG/ML Medicated Liquid Soap
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Sunburst Chemicals, Inc.
    Dosage Form:
    Soap - Any compound of one or more fatty acids, or their equivalents, with an alkali; soap is detergent and is much employed in liniments, enemas, and in making pills. It is also a mild aperient, antacid and antiseptic.
    Administration Route(s):
  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
    • Active Ingredient(s):
  • CHLOROXYLENOL 7.5 mg/mL
    • Sample Package:
    No
    FDA Application Number:
    505G(a)(3)
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    02-14-2008
    End Marketing Date:
    06-30-2024
    Exclude Flag:
    N
    Code Structure:

    The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 63621-353-65?

    The NDC Packaged Code 63621-353-65 is assigned to a package of 8 bag in 1 box / 1000 ml in 1 bag of Sundrops 67, a human over the counter drug labeled by Sunburst Chemicals, Inc.. The product's dosage form is soap and is administered via topical form.

    Is NDC 63621-353 included in the NDC Directory?

    Yes, Sundrops 67 with product code 63621-353 is active and included in the NDC Directory. The product was first marketed by Sunburst Chemicals, Inc. on February 14, 2008.

    What is the 11-digit format for NDC 63621-353-65?

    The 11-digit format is 63621035365. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

    This package code is originally configured in a 5-3-2 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

    10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
    5-3-263621-353-655-4-263621-0353-65